Acalabrutinib FDA approved for the treatment of pre-treated MCL

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FDA ONCOLOGY & HAEMATOLOGY APPROVALS

Acalabrutinib FDA approved for treatment of adult patients with pre-treated mantle cell lymphoma

By: News Feed | Last updated: 31st October 2017 | In: US FDA Onc\Haem Approvals

Article Keywords

acalabrutinib, Acerta Pharma, AstraZeneca, AZ, Calquence, FDA, lymphoma, MCL

On 31 October 2017, the FDA granted accelerated approval to acalabrutinib (Calquence®, AstraZeneca under license of Acerta Pharma BV) for treatment of adult patients with mantle cell lymphoma (MCL) and pre-treated with one or more prior therapy.

Disclaimer

This article is not medical advice. Patients should seek personal assessment by a licenced specialist. Physicians are recommended to read the full publication(s) as cited in the article before making medical decisions. This article does not supersede nor replace the published article(s).

© Copyright 2018 MediPaper Medical Communications Ltd.

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